Fyxis associated with two missense point mutations in its gene and can be detected by PCR–SSP
By: C. Gassner, R.L. Kraus, T. DOVC, S. KILGA-NOGLER, I. UTZ, T.H. MUELLER, F. SCHUNTER and D. SCHOENITZER
Paid access
|Oct 2020Authors
C. Gassner
Basel Institute for Immunology/Labor 11, Basel, Switzerland
R.L. Kraus
Institut fuer Biochemische Pharmakologie, University of Innsbruck, Innsbruck, Austria
T. DOVC
Dept.of Immunohematology, Blood Transfusion Centre of Slovenia, Ljubljana, Slovenia
S. KILGA-NOGLER
Central Institute for Blood Transfusion and Immunological Department, General and University Hospital of Innsbruck, Innsbruck, Austria
I. UTZ
Central Institute for Blood Transfusion and Immunological Department, General and University Hospital of Innsbruck, Innsbruck, Austria
T.H. MUELLER
German Red Cross Blood Center, Oldenburg, Germany
F. SCHUNTER
German Red Cross Blood Center Oldenburg, Oldenburg, Germany
D. SCHOENITZER
Central Institute for Blood Transfusion and Immunological Department, General and University Hospital of Innsbruck, Innsbruck, Austria
DOI: https://doi.org/10.21307/immunohematology-2019-579 | Journal eISSN: 1930-3955 | Journal ISSN: 0894-203X
Language: English
Page range: 61 - 67
Published on: Oct 18, 2020
Published by: American National Red Cross
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2020 C. Gassner, R.L. Kraus, T. DOVC, S. KILGA-NOGLER, I. UTZ, T.H. MUELLER, F. SCHUNTER, D. SCHOENITZER, published by American National Red Cross
This work is licensed under the Creative Commons License.